Director, Engineering

MSD

Closes in 7 days Remote

Quick summary

Work type
Remote
Location
Remote
Salary
$173,200–$272,600 / yr
Posted
7 days ago
Closes
Jun 24, 2026 (soon)

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $217k
This role $223k
$160k most similar roles pay here $287k

This role pays less than 54% of similar roles. Most pay $172,500–$262,200 — the shaded band above. At the midpoint, this role pays about $223k versus about $217k for comparable roles.

Based on 239 similar postings.

Employer

About MSD

MSD (Merck Sharp & Dohme) is the international name for Merck & Co., a major U.S.-based pharmaceutical company.

MSD currently has 11 open roles on FindRole.

Listed pay typically runs $117,000–$184,200 across 11 roles with salary data.

Most-posted roles

View all roles at MSD

At a glance

TL;DR · Director, Engineering

The Development and Commercialization Team (DCT) leader is a senior-level role responsible for advancing the company’s biologics portfolio by delivering robust CMC strategies from early development to commercial manufacturing. This includes managing end-to-end execution of DCT deliverables, fostering a collaborative environment, mitigating risks across technical, operational, and regulatory factors, and ensuring compliance with global standards. The ideal candidate will have extensive experience in biopharmaceutical development and commercialization, deep technical expertise, and the ability to navigate ambiguity while driving innovative solutions. Key skills include strategic thinking, problem-solving, and strong communication abilities, along with a background in chemical process development, GMP compliance, and manufacturing scale-up. This role demands a leader who can effectively manage cross-functional teams and deliver high-quality outcomes within a fast-paced environment.

What you'll do

  • Lead the DCT team to deliver on-time execution of CMC development and commercialization strategies.
  • Ensure robust processes, analytics, and control strategies for seamless tech transfer and regulatory approval.
  • Analyze risks and develop innovative solutions to mitigate technical, operational, and regulatory challenges.
  • Represent CMC in governance bodies, influencing stakeholders to ensure a balanced approach between speed, cost, and robustness.
  • Comply with global regulations and execute cGMP practices throughout product development and commercialization.

What we're looking for

  • Demonstrated expertise in technical aspects and interdependencies across DS, DP, Device, Packaging, Analytical, Regulatory, Quality, and Supply Chain.
  • Deep understanding of connectivity between clinical, CMC, and HH to successfully launch new products.
  • Strong cross-divisional networking skills with experience in commercializing multiple large molecule programs.
  • Expert knowledge in global regulatory requirements for large molecule commercialization and BLA assembly.
  • Proven ability to lead high-performing teams, drive accountability, and deliver on-time project execution.
  • Strategic thinking and innovative problem-solving skills to navigate ambiguity and uncertainty effectively.
  • Strong collaborative skills with the ability to work strategically at all levels of management.

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